P
US7534561B2ExpiredUtilityPatentIndex 97

Nucleic acid array in situ fabrication methods and arrays produced using the same

Assignee: AGILENT TECHNOLOGIES INCPriority: Apr 2, 2003Filed: Apr 2, 2003Granted: May 19, 2009
Est. expiryApr 2, 2023(expired)· nominal 20-yr term from priority
Inventors:SANA THEODORE RLEPROUST ERIC MPERBOST MICHEL G MWOLBER PAUL K
C12Q 1/6837B01J 2219/00689B01J 2219/00612B01J 2219/0036B82Y 30/00C40B 60/14B01J 2219/00659B01J 2219/00378B01J 2219/00695B01J 2219/00626B01J 2219/00707C40B 50/14B01J 2219/00608B01J 2219/00722B01J 2219/00596B01J 2219/00637B01J 2219/00585B01J 2219/00675C40B 40/06B01J 2219/00693B01J 2219/0061B01J 2219/00529B01J 2219/0059B01J 19/0046
97
PatentIndex Score
95
Cited by
42
References
14
Claims

Abstract

Methods and devices for producing a nucleic acid arrays using in situ nucleic acid array synthesis protocols are provided. A feature of certain embodiments of the invention is that control probes are produced in collections of features, e.g., columns, of the arrays that have been selected according to a particular efficient control probe feature/column selection protocol. A feature of certain other embodiments of the invention is that an “all-bases-all-layers” probe set is produced in at least one of column of the arrays. Also provided are devices configured for use in the subject methods, as well as arrays produced using the subject methods and devices as well as methods for using such arrays.

Claims

exact text as granted — not AI-modified
1. A method of producing a nucleic acid microarray comprising two or more different nucleic acids immobilized at different locations on a surface, said method comprising:
 (a) identifying a collection of feature locations of the nucleic acid microarray in which to produce control probes during synthesis of the nucleic acid microarray using an in situ microarray synthesis protocol, wherein said protocol utilizes a pulse-jet fluid deposition device having a total number of nozzle groups Y that traverse an entire array surface in one or more passes during said protocol, wherein each pass of said protocol is made up of a total number of swaths Z, and wherein said collection of feature locations samples less than all of said nozzle groups Y in any given swath but all of said nozzle groups Y in said total number of swaths Z of any given pass; and 
 (b) producing said nucleic acid microarray using said in situ microarray synthesis protocol, wherein said control probes are produced in said collection of feature locations. 
 
     
     
       2. The method according to  claim 1 , wherein said collection of feature locations is made up of a collection of columns. 
     
     
       3. The method according to  claim 1 , wherein said collection of feature locations make up a regular pattern. 
     
     
       4. The method according to  claim 1 , wherein said collection of feature locations make up a random pattern. 
     
     
       5. The method according to  claim 1 , wherein less than about 50% of the total number of groups Y is sampled in any given swath. 
     
     
       6. The method according to  claim 1 , wherein the same collection of feature locations is employed for printing control probes in each pass of said protocol. 
     
     
       7. A method for producing a nucleic acid microarray having a nucleic acid microarray layout, wherein said nucleic acid microarray comprises test probes and control probes, and wherein said method comprises:
 (a) selecting a collection of columns of said nucleic acid microarray layout in which to produce said control probes during synthesis of said nucleic acid microarray using an in situ microarray synthesis protocol, wherein said nucleic acid microarray layout has a total number of columns X and said in situ microarray synthesis protocol utilizes a pulse-jet fluid deposition device having a total number of nozzle groups Y, and wherein said selecting comprises
 identifying a column pattern period that either:
 (i) shares no prime factors with Y and when multiplied by Y produces a product that does not exceed X; or 
 (ii) shares a single prime factor of 2 with Y and when multiplied by Y produces a product that does not exceed X; 
 
 employing said column pattern period to select said collection of columns of said nucleic acid microarray layout in which to produce said control probes; and 
 
 (b) producing said nucleic acid microarray using said in situ microarray synthesis protocol, wherein said control probes are produced in said collection of columns. 
 
     
     
       8. The method according to  claim 7 , wherein said pattern period shares no prime factors with Y. 
     
     
       9. The method according to  claim 7 , wherein said method further comprises selecting an initial column in which to print control probes that results in control probes being printed in substantially the same number of replicate columns per nozzle group. 
     
     
       10. The method according to  claim 7 , wherein said pattern period shares a single prime factor of 2 with Y. 
     
     
       11. The method according to  claim 10 , wherein said employing comprises selecting a first collection of columns in which to print control probes and then a second collection of columns in which to print control probes, wherein said second collection of columns has an initial column that is adjacent to the initial column of said first collection of columns. 
     
     
       12. The method according to  claim 7 , wherein Y is an integer ranging from about 5 to about 50. 
     
     
       13. The method according to  claim 7 , wherein X is an integer ranging from about 50 to about 1024. 
     
     
       14. The method according to  claim 7 , wherein each nozzle group making up said total number Y is made up of 6 individual nozzles.

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